N-(6-Bromo-5-fluoro-2-methylpyridin-3-yl)methanesulfonamide CAS 2643341-06-2

Purity 97%+In StockPharmaceutical Standards
CAS No.2643341-06-2
Molecular FormulaC7H8BrFN2O2S
Molecular Weight283.12 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(6-Bromo-5-fluoro-2-methylpyridin-3-yl)methanesulfonamide CAS 2643341-06-2 chemical structure

Description

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

CATO supplies N-(6-Bromo-5-fluoro-2-methylpyridin-3-yl)methanesulfonamide (CAS 2643341-06-2), a certified reference material (molecular formula C7H8BrFN2O2S, MW 283.12 g/mol) for analytical method development and quality control.

The molecular framework of N-(6-Bromo-5-fluoro-2-methylpyridin-3-yl)methanesulfonamide (C7H8BrFN2O2S) is characterized by an amide group, a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, fluorine/bromine substitution, an aromatic ring system. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

CATO manufactures N-(6-Bromo-5-fluoro-2-methylpyridin-3-yl)methanesulfonamide under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC7H8BrFN2O2S
Molecular Weight283.12 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2002
Halogen ContentF/Br-containing
Nitrogen Atoms2
Sulfur Atoms1

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